Perennial plants growing at high latitudes synchronize growth and dormancy to appropriate seasons by sensing environmental cues. Autumnal growth cessation, bud set and dormancy induction are commonly driven by the length of photoperiod and light quality, and the responses are modified by temperature. However, although ultraviolet (UV)-B radiation is well known to affect plant growth and development, information on the effects on bud phenology is scarce. We examined the separate and combined effects of enhanced temperature and UV-B on autumnal bud set and spring bud break in female and male clones of Populus tremula in an outdoor experiment in Joensuu, Eastern Finland. Enhancements of UV-B and temperature were modulated to +30% and +2 °C, respectively, from June to October 2012. Enhanced UV-B accelerated bud set, while increased temperature delayed it. For both UV-B and temperature, we found sex-related differences in responsiveness. Temperature increase had a stronger delaying effect on bud maturation in male compared with female clones. Also, male clones were more responsive to UV-B increase than female clones. Increasing autumnal temperature enhanced bud break in spring for both sexes, while UV-B enhanced bud break in male clones. In conclusion, we found that UV-B affected phenological shifts in P. tremula, and that temperature and UV-B affected genders differently.

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The effects of warming on autumnal growth cessation and bud formation in trees remain ambiguous due to contrasting observations between a range of studies under controlled conditions and field experiments. High night temperature has been reported to advance growth cessation and bud formation in several tree species grown under controlled conditions. On the other hand, some recent field experiments have shown that autumn warming delays bud formation, although the temperature parameters that could account for this effect have not been identified. In addition, dioecious species have been shown to respond differently to environmental change, and differential warming effects on the sexes have received limited attention, even more so in relation to phenology. In a data set including three separate field experiments employing either experimental warming or an elevational gradient, we tested the effect of different temperature parameters on apical, vegetative bud formation and transitions between bud stages in female and male clones of Eurasian aspen (Populus tremula). Increased temperature was found to delay bud formation, and this process was best explained by maximum daily temperature. Males were significantly delayed compared with females in forming green closed buds, a process best explained by mean 24 h temperature. Bud maturation was best explained by mean daytime temperature, and buds matured significantly faster in males than in females, possibly explaining why females and males did not differ in terms of overall bud formation. In conclusion, our data show that delayed bud formation in Eurasian aspen during autumn can be attributed to the effect of high temperature, and this effect is in contrast to most of the evidence from studies of bud development in controlled environments.

Light and temperature are crucial factors for the annual growth rhythm of tree seedlings of the boreal and temperate zone. Dormant, vegetative winter buds are formed under short days (SD) and altered light quality. In the conifer Norway spruce, expression of FTL2 increases and PaCOL1-2 and PaSOC1 decrease under light regimes, inducing bud set. Although temperature is known to modulate the timing of bud set, information about combined effects of light climate and temperature on bud phenology and gene expression is limited. We studied the interactive effects of temperature (18, 22/24 °C) and day extension with blue (B), red (R) or far-red (FR) light or different R:FR ratios compared to SD on growth–dormancy cycling and expression of FTL2, PaCOL1-2 and PaSOC1 in Norway spruce seedlings. Day-extension with B light and all treatments involving FR light sustained shoot elongation, with increased growth at higher temperature. The R light treatment resulted in delayed/prevented bud set compared to SD, with more delay/prevented bud set at 24 °C than 18 °C. This was associated with lower PaFTL2-transcript levels at 24 °C and more rapid subsequent bud burst. For the growth-sustaining treatments (long days, FR and B light), the PaFTL2-transcript levels were generally lower and those of PaCO1-2 and PaSOC1 higher compared with SD and R light. In conclusion, our results demonstrate more reduced/prevented bud set and faster bud burst with increased temperature under day extension with R light, indicating less deep dormancy than at lower temperature. Also, sustained shoot elongation under the B light treatment (27 µmol m−2 s−1) in contrast to the lower B light-irradiances tested previously (≤ 13 µmol m−2 s−1), demonstrates an irradiance-dependent effect of day extension with B light.

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